State

New Jersey product recalls

73,741 recalls have nationwide distribution and so reach New Jersey. 9,780 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,780
Critical: 1,246
Severe: 2,942
Most recent: 2026-10-28

Of the 9,780 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,942 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,780 recalls whose distribution notice names New Jersey specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33551–33575 of 83521

SevereFDA (Drugs)·D-1016-2020·2020-03-25
Perrigo Recalls Ranitidine Tablets Due to Possible N-Nitrosodimethylamine Contamination
Perrigo Company PLC is recalling specific lots of Regular Strength Acid Reducer Ranitidine tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.
Product
Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 160 tablets per bottle. [NDC: Brand] NDC CVS Health.: 69842-293-06
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1018-2020·2020-03-25
Perrigo Recalls Ranitidine Tablets Due to Potential N-Nitrosodimethylamine Contamination
Perrigo Company PLC is recalling Maximum Strength Acid Reducer Ranitidine tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.
Product
Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 24 tablets per bottle. [Brand, NDC] NDC Being Well: 46994-852-62; NDC Care One 41520-392-02; NDC CVS Health: 59779-540-02; NDC DG Health: 55910-852-02; NDC Equaline: 41163-852-62; NDC Equate: 49035-608-02; NDC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1521-2020·2020-03-25
Avid Medical Recalls Custom Procedure Trays Due to Sterility Concerns
Avid Medical, Inc. is recalling 628 custom procedure trays because they contain surgical gowns that may not be sterile. This poses a risk of surgical site infection and cross-contamination.
Product
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multiple item and lot numbers.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1502-2020·2020-03-25
Agfa DR 800 X-Ray System Recalled for Tomosynthesis Sequence Error
Agfa N.V. is recalling two DR 800 X-ray systems because the tomosynthesis image acquisition sequence did not stop automatically after the expected number of exposures.
Product
AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Product Usage: TomoSynthesis is used to synthesize tomographic slices from a single tomographic sweep. The DR 800 is not intended for mammography applications
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2020·2020-03-25
Avid Medical Recalls Custom Procedure Trays Due to Sterility Concerns
Avid Medical, Inc. is recalling 1,906 custom procedure trays because they contain surgical gowns that may not be sterile, posing a risk of surgical site infection.
Product
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multiple item and lot numbers.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1524-2020·2020-03-25
Medtronic CareLink 2090 Programmer Recalled for Cyber Vulnerabilities
Medtronic is recalling 23,180 CareLink 2090 Programmer devices worldwide due to improper access control and cleartext transmission of sensitive information.
Product
Medtronic CareLink 2090 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as pacemaker/ICD/CRT.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V178000·2020-03-25
Thor Motor Coach motorhomes recalled for faulty rear axle differential
Thor Motor Coach is recalling certain 2020-2021 motorhomes due to insufficient rear axle differential fluid that could cause driveshaft separation and loss of vehicle drive, increasing crash risk.
Product
THOR MOTOR COACH — THOR MOTOR COACH VEGAS, AXIS, CHATEAU, FOUR WINDS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1498-2020·2020-03-25
LivaNova Heater-Cooler System 3T Recalled for NTM Contamination Risk
LivaNova is recalling Heater-Cooler System 3T units to reduce the risk of NTM contamination by providing validated cleaning and disinfection instructions.
Product
LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T System is used to circulate water through heat exchangers to warm or cool a patient during cardiopulmonary bypass procedures lasting 6 hours or less.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1522-2020·2020-03-25
Avid Medical Recalls Custom Procedure Trays Containing Non-Sterile Gowns
Avid Medical is recalling 2,632 custom procedure trays because they contain surgical gowns that may not be sterile, posing a risk of surgical site infection.
Product
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multiple item and lot numbers.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1497-2020·2020-03-25
Siemens Artis Angiography Systems Recalled for Software Movement Blockage
Siemens is recalling Artis angiography systems because a software issue could block stand and table movements.
Product
Artis zee Biplane, Model No. 10094141; Artis zee Ceiling, Model No. 10094137; Artis zee Floor, Model No. 10094135; Artis zeego, Model No. 10280959 Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2020·2020-03-25
Avid Medical Recalls Custom Procedure Trays Due to Sterility Concerns
Avid Medical, Inc. is recalling 1,644 custom procedure trays because they contain surgical gowns that may not be sterile, posing a risk of surgical site infection.
Product
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multiple item and lot numbers.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1480-2020·2020-03-25
Aesculap Recalls Columbus Knee Implant Components Due to LDPE Particles
Aesculap Implant Systems LLC is recalling Columbus knee implant components because low-density polyethylene particles may be present on the surface when the packaging is opened.
Product
COLUMBUS CRA/PSA TIB.PLAT.CEMENTED, Knee implant components, various sizes, model nos. NN469K NN470K NN471K NN472K NN473K NN474K NN475K NN476K NN477K NN478K NN479K Product Usage: Tibia-Plateaus are part of implants in the group of knee endoprosthetics. For these…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0837-2020·2020-03-25
Dreyers Outshine Strawberry Fruit Bars Recalled for Plastic Contamination
Dreyers Grand Ice Cream is recalling Outshine Strawberry Fruit Bars due to consumer complaints of white plastic pieces.
Product
Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl. oz. (435 mL) UPC: 041548610047 Case UPC: 10041548610044
Category
Food
Distribution
39 states
HighFDA (Devices)·Z-1519-2020·2020-03-25
Avid Medical Recalls Custom Procedure Trays Due to Sterility Concerns
Avid Medical is recalling 230 custom procedure trays because they contain surgical gowns that may not be sterile, posing a risk of surgical site infection.
Product
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multiple item and lot numbers.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1514-2020·2020-03-25
Siemens IMMULITE 2000 Estradiol Test Kits Recalled for High Discordant Results
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Estradiol test kits due to high discordant results that may lead to misinterpretation of patient menopausal status.
Product
IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 tests) and L2KE26(D) (600 tests) and OUS: L2KE22 (200 tests), L2KE26 (600 tests) - Product Usage: For in vitro diagnostic use with the IMMULITE systems Analyzers for the quantitative measurement of estradiol in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1512-2020·2020-03-25
Boston Scientific DYNAGEN EL ICD DR Recall for Unapproved Software
Boston Scientific is recalling one DYNAGEN EL ICD DR device because a software update downloaded unapproved applications to four programmers.
Product
Boston Scientific, Implantable Cardioverter Defibrillator, DYNAGEN EL ICD DR, Model D152 - Product Usage: Implantable cardioverter defibrillators (ICDs) are intended to provide ventricular anti-tachycardia pacing (ATP) and ventricular defibrillation for automated treatment of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1495-2020·2020-03-25
Siemens Artis Q Angiography Systems Recalled for Software Movement Issue
Siemens is recalling Artis Q angiography systems because a software issue could block stand and table movements.
Product
Artis Q Biplane, Model No. 10848282; Artis Q Ceiling, Model No.10848281; Artis Q Floor, Model No. 10848280; Artis Q zeego, Model No. 10848283 Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1523-2020·2020-03-25
Avid Medical Recalls Custom Procedure Trays Due to Sterility Concerns
Avid Medical is recalling 5,004 custom procedure trays because they contain surgical gowns that may not be sterile, posing a risk of surgical site infection.
Product
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multiple item and lot numbers.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1501-2020·2020-03-25
Siemens Ysio X-Ray System Recalled for Unexpected Tube Stand Movement
Siemens is recalling Ysio X-Ray systems because a software error may cause the ceiling tube stand to move unexpectedly when activated by the user.
Product
Ysio, model no. 10281013 Product Usage: The product is a stationary X-Ray system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V179000·2020-03-25
Gillig Recalls 2012-2020 Low Floor Buses Due to Fire Risk
Gillig is recalling 8,224 Low Floor buses because improper circuit breaker ratings may increase the risk of a fire.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2020·2020-03-25
Avid Medical Recalls Custom Procedure Trays Due to Sterility Concerns
Avid Medical is recalling 21,326 custom procedure trays because they contain surgical gowns that may not be sterile, posing a risk of surgical site infection.
Product
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multiple item and lot numbers.
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1481-2020·2020-03-25
Aesculap Recalls Knee Implant Components Due to Potential LDPE Particles
Aesculap Implant Systems LLC is recalling specific knee implant components because low-density polyethylene particles may be present on the surface upon opening.
Product
AS COLUMBUS CR/PS TIB.PLAT.CEMENTED,Knee implant components, various sizes, model nos. NN058Z NN070Z NN071Z NN072Z NN073Z NN074Z NN075Z NN076Z NN077Z NN078Z NN079Z NN470Z NN471Z NN472Z NN473Z NN474Z NN475Z NN476Z NN477Z NN478Z NN479Z Product Usage…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2020·2020-03-25
Aesculap Recalls Knee Implants Due to Potential LDPE Particles
Aesculap Implant Systems LLC is recalling specific knee implant components because low density polyethylene particles may be present on the surface.
Product
COLUMBUS REV F TIBIA OFFSET CEMENTED, Knee implant components, various sizes, model nos. NR068K NR068Z NR070K NR070Z NR071K NR071Z NR072K NR072Z NR073K NR073Z NR074K NR074Z NR075K NR075Z NR076K NR076Z NR077K NR077Z NR078K NR078Z NR079K NR079Z Product…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0838-2020·2020-03-25
Outshine Pineapple Fruit Bars Recalled for White Plastic Pieces
Dreyers Grand Ice Cream is recalling Outshine Pineapple Fruit Bars due to consumer complaints of white plastic pieces in the product.
Product
Outshine Fruit Bars Pineapple; 6 Fruit Ice Bars; 6x2 5 fl. oz) 14.7 Fl. oz. (435 mL); Package UPC: 041548750958; Case UPC: 10041548750955
Category
Food
Distribution
39 states
HighFDA (Devices)·Z-1479-2020·2020-03-25
Aesculap Recalls Columbus Knee Implant Components Due to LDPE Particles
Aesculap Implant Systems LLC is recalling Columbus CR/PS Tibial Plateau knee implant components because low-density polyethylene particles may be present on the surface.
Product
COLUMBUS CR/PS TIB.PLAT.PLASMAPORE, Knee implant components, various sizes, model nos. NN081K NN082K NN083K NN084K NN085K NN086K NN087K NN088K NN089K Product Usage: Tibia-Plateaus are part of implants in the group of knee endoprosthetics. For these implant parts there…
Category
Medical Device
Distribution
Distributed nationwide